Synthesis of the phorboxazoles—potent, architecturally novel marine natural products
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology
Link
http://www.nature.com/articles/ja20168.pdf
Reference53 articles.
1. Searle, P. A. & Molinski, T. F. Phorboxazoles A and B: potent cytostatic macrolides from marine sponge Phorbas species. J. Am. Chem. Soc. 117, 8126–8131 (1995).
2. Searle, P. A., Molinski, T. F., Brzezinski, L. J. & Leahy, J. W. Absolute configuration of phorboxazoles A and B from the marine sponge Phorbas sp. 1. Macrolide and hemiketal rings. J. Am. Chem. Soc. 118, 9422–9423 (1996).
3. Molinski, T. F. Absolute configuration of phorboxazoles A and B from the marine sponge, Phorbas sp. 2. C43 and complete stereochemistry. Tetrahedron Lett. 37, 7879–7880 (1996).
4. Molinski, T. F., Brzezinski, L. J. & Leahy, J. W. Absolute configuration of phorboxazole A C32-C43 analogs by CD exciton-coupling of allylic 2-naphthoate esters. Tetrahedron Asymmetry 13, 1013–1016 (2002).
5. Capon, R. J. et al. Esmodil: an acetylcholine mimetic resurfaces in a southern Australian marine sponge Raspailia (Raspailia) sp. Nat. Prod. Res. 18, 305–309 (2004).
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